(Q80998833)

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Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases

scientific article published on 01 November 2004

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scholarly article

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5 January 2020

Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases (English)

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Europe PubMed Central

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5 January 2020

Phillip D. Whitfield

5

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5 January 2020

8

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5 January 2020

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John J Hopwood

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5 January 2020

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Steven L Ramsay

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5 January 2020

Irene Maire

2

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5 January 2020

Colleen Bindloss

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5 January 2020

Maria Fuller

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5 January 2020

Monique Piraud

6

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5 January 2020

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1 November 2004

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5 January 2020

Molecular Genetics and Metabolism

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5 January 2020

83

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5 January 2020

3

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5 January 2020

231-238

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5 January 2020

Lysosomal disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Correlation among genotype, phenotype, and biochemical markers in Gaucher disease: implications for the prediction of disease severity

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometry.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Altered trafficking and turnover of LAMP-1 in Pompe disease-affected cells.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Urinary excretion of sulphated N-acetylhexosamines in patients with various mucopolysaccharidoses

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

Prenatal diagnosis of lysosomal storage diseases.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.015

7 January 2021

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10.1016/J.YMGME.2004.07.015

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Europe PubMed Central

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5 January 2020

PubMed publication ID

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5 January 2020

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